Does BOTULINUM TOXIN TYPE A Cause Liver function test increased? 356 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 356 reports of Liver function test increased have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 9.5% of all adverse event reports for BOTULINUM TOXIN TYPE A.
356
Reports of Liver function test increased with BOTULINUM TOXIN TYPE A
9.5%
of all BOTULINUM TOXIN TYPE A reports
356
Deaths
287
Hospitalizations
How Dangerous Is Liver function test increased From BOTULINUM TOXIN TYPE A?
Of the 356 reports, 356 (100.0%) resulted in death, 287 (80.6%) required hospitalization, and 289 (81.2%) were considered life-threatening.
Is Liver function test increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 356 reports have been filed with the FAERS database.
What Other Side Effects Does BOTULINUM TOXIN TYPE A Cause?
Off label use (1,785)
Drug ineffective (1,175)
Drug intolerance (1,004)
Product use in unapproved indication (950)
Headache (797)
Migraine (775)
Maternal exposure during pregnancy (716)
Pain (714)
Hypoaesthesia (703)
Nausea (665)
What Other Drugs Cause Liver function test increased?
METHOTREXATE (3,839)
ADALIMUMAB (2,070)
ETANERCEPT (1,829)
LEFLUNOMIDE (1,521)
ABATACEPT (1,415)
TOCILIZUMAB (1,406)
RITUXIMAB (1,325)
SULFASALAZINE (1,263)
HYDROXYCHLOROQUINE (1,259)
TOFACITINIB (1,221)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Liver function test increased Risk?
BOTULINUM TOXIN TYPE A vs BREMELANOTIDE
BOTULINUM TOXIN TYPE A vs BRENTUXIMAB
BOTULINUM TOXIN TYPE A vs BRENTUXIMAB VEDOTIN
BOTULINUM TOXIN TYPE A vs BREO ELLIPTA
BOTULINUM TOXIN TYPE A vs BREXANOLONE